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公开(公告)号：US06143745A
公开(公告)日：2000-11-07
申请号：US171524
申请日：1998-10-21
申请人： Karl Eicken , Eberhard Ammermann , Siegfried Strathmann , Gisela Lorenz , Harald Kohle , Gunter Retzlaff
发明人： Karl Eicken , Eberhard Ammermann , Siegfried Strathmann , Gisela Lorenz , Harald Kohle , Gunter Retzlaff
摘要： Compositions for controlling harmful fungi, containing in a solid or liquid carrier pyridaben of the formula: ##STR1## or fenpyroximate of the formula: ##STR2## or tebufenpyrad of the formula: ##STR3## and at least one amide compound of the following formula I:A--CO--NR.sup.1 R.sup.2 (I)where the substituents have the meanings indicated in the description, and methods for controlling harmful fungi using compositions of this type are described.
摘要翻译： PCT No.PCT / EP97 / 02037 371日期：1998年10月21日 102（e）日期1998年10月21日PCT 1997年4月22日PCT PCT。 公开号WO97 / 39630 PCT 日期1997年10月30日用于控制有效真菌的组合物，其含有下式的固体或液体载体哒哒啶：下式的咪苯并哒嗪或下式的替泊芬吡啶：和至少一种下式I的酰胺化合物：A-CO -NR1R2（I）其中取代基具有说明书中指出的含义，并且描述了使用这种类型的组合物来控制有害真菌的方法。
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公开(公告)号：US6130224A
公开(公告)日：2000-10-10
申请号：US29629
申请日：1998-03-04
申请人： Karl Eicken , Harald Kohle , Gunter Retzlaff , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Karl Eicken , Harald Kohle , Gunter Retzlaff , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
CPC分类号： A01N43/54
摘要： The present invention relates to composiitons for controlling harmful fungi which comprise, as active ingredients, fenazaquin and at least one amide compound of the formula IA--CO--NR.sup.1 R.sup.2 Iwhere A, R.sup.1 and R.sup.2 have the meanings given in the description. The compositions according to the invention are particularly useful for controlling botrytis.
摘要翻译： PCT No.PCT / EP96 / 03861 Sec。 371日期：1998年3月4日 102（e）1998年3月4日PCT PCT 1996年9月5日PCT公布。 公开号WO97 / 08952 日期1997年3月13日本发明涉及用于控制有害真菌的组合物，其包含作为活性成分的灭草醌和至少一种式I A-CO-NR1R2I的酰胺化合物，其中A，R 1和R 2具有在说明书中给出的含义 。 根据本发明的组合物特别可用于控制葡萄孢菌。
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3.发明授权Fungicidal mixtures based on amide compounds and morpholine or piperidine derivatives 有权基于酰胺化合物和吗啉或哌啶衍生物的杀真菌混合物公开(公告)号：US08530380B2
公开(公告)日：2013-09-10
申请号：US11322211
申请日：2005-12-30
申请人： Klaus Schelberger , Maria Scherer , Karl Eicken , Manfred Hampel , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Klaus Schelberger , Maria Scherer , Karl Eicken , Manfred Hampel , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
CPC分类号： A01N43/40 , A01N47/34 , A01N47/12 , A01N43/76 , A01N43/08 , A01N37/46 , A01N37/38 , A01N37/36 , A01N2300/00
摘要： Fungicidal mixtures comprise as active components a) an amide compound of the formula I A-CO—NR1R2 I in which A, R1 and R2 are as defined in the description, and b) dimethomorph or flumetover, and/or c) a valinamide of the formula III in which R13 is C3-C4-alkyl and R14 is naphthyl or phenyl, where the phenyl radical is substituted in the 4-position by a halogen atom, a C1-C4-alkyl or C1-C4-alkoxy group, and/or d) benalaxyl, ofurace, metalaxyl, furalaxyl or oxydixyl, and/or e) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea in a synergistically effective amount.
摘要翻译： 杀真菌混合物包含作为活性组分的a）式I A-CO-NR1R2I的酰胺化合物，其中A，R 1和R 2如说明书中所定义，和b）烯酰吗啉或灭火剂，和/或c）缬氨酰胺 式中R 13为C 3 -C 4 - 烷基，R 14为萘基或苯基，其中苯基在4-位被卤素原子取代，C 1 -C 4 - 烷基或C 1 -C 4 - 烷氧基，和/ 或d）苯菌灵，海藻，甲霜灵，furalaxyl或oxydixyl，和/或e）1-（2-氰基-2-甲氧基亚氨基乙酰基）-3-乙基脲以协同有效量。
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4.发明授权Fungicide mixtures which are based on derivatives of morpholine or piperidine and derivatives oxime ether 失效基于吗啉或哌啶衍生物和衍生物肟醚的杀菌剂混合物公开(公告)号：US07026315B1
公开(公告)日：2006-04-11
申请号：US09868515
申请日：1999-12-11
申请人： Klaus Schelberger , Maria Scherer , Reinhold Saur , Karl Eicken , Egon Haden , Eberhard Ammermann , Thomas Grote , Gisela Lorenz , Siegfried Strathmann
发明人： Klaus Schelberger , Maria Scherer , Reinhold Saur , Karl Eicken , Egon Haden , Eberhard Ammermann , Thomas Grote , Gisela Lorenz , Siegfried Strathmann
IPC分类号： A61K31/535 , A61K31/15 , A61K31/165 , A61K31/435 , A61K31/335
摘要： Fungicidal mixtures, comprising as active components a) a morpholine or piperidine derivative I selected from the group of the compounds Ia, Ib, Ic and Id and b) compounds of the formula II in a synergistically effective amount are described.
摘要翻译： 包含作为活性组分的杀真菌混合物a）描述了选自化合物Ia，Ib，Ic和Id的吗啉或哌啶衍生物I和b）协同有效量的式II化合物。
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5.发明申请Novel benzyl amidoxime derivatives, intermediate products and method for their production and use as fungicides 失效新型苄基偕胺肟衍生物，其生产和使用的中间产物和方法作为杀真菌剂公开(公告)号：US20050187265A1
公开(公告)日：2005-08-25
申请号：US11061470
申请日：2005-02-22
申请人： Joachim Rheinheimer , Karl Eicken , Ingo Rose , Thomas Grote , Eberhard Ammermann , John-Bryan Speakman , Siegfried Strathmann , Gisela Lorenz
发明人： Joachim Rheinheimer , Karl Eicken , Ingo Rose , Thomas Grote , Eberhard Ammermann , John-Bryan Speakman , Siegfried Strathmann , Gisela Lorenz
IPC分类号： A61P31/10 , A01N37/52 , A61K31/165 , C07C259/14 , C07D333/22 , A61K31/381 , A61K31/415 , A61K31/44 , C07C259/10
CPC分类号： C07C259/14 , A01N37/52 , C07C2601/02
摘要： Novel benzamidoxime derivatives, processes and intermediates for their preparation and their use as fungicides are described. In the context of the present invention, benzamidoxime derivatives are compounds of the formula I where: A is an aryl or hetaryl radical; Y is a straight-chain or branched C1-C4-alkylene group, where one carbon can be replaced by oxygen, nitrogen or sulfur or by a cyclopropyl group; Rn1 are one to five identical or different radicals from the group consisting of: hydrogen, halogen, C1-C6-alkyl, C1-C6-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylthio, C1-C4-alkoxyalkoxy; R2 is unsubstituted or substituted phenyl-C1-C6-alkyl, thienyl-C1-C4-alkyl, or pyrazolyl-C1-C4-alkyl, Rp3 are one to five identical or different radicals from the group consisting of: hydrogen, halogen, C1-C6-alkyl, C1-C6-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylthio, C1-C4-alkoxyalkoxy, C1-C6-alkylcarbonyl; n is 0-5; p is, depending on the number of free valencies, 0-4.
摘要翻译： 描述了新的苯甲酰胺肟衍生物，其制备方法和中间体及其作为杀真菌剂的用途。 在本发明的上下文中，苯甲酰胺肟衍生物是式I的化合物，其中：A是芳基或杂芳基; Y是直链或支链C 1 -C 4 - 亚烷基，其中一个碳可被氧，氮或硫取代或被环丙基取代; R 1是与以下组成的组中的一至五个相同或不同的基团：氢，卤素，C 1 -C 6 C 1 -C 6烷基，C 1 -C 6 - 烷氧基，C 1 -C 4 - 卤代烷基 ，C 1 -C 4 - 卤代烷氧基，C 1 -C 4 - 烷硫基，C 1 -C 4 - 烷氧基烷氧基; R 2是未取代或取代的苯基-C 1 -C 6 - 烷基，噻吩基-C 1 -C 或 - 吡唑基-C 1 -C 4 - C 1-4 - 烷基，R 3 - （CH 3）3 - / SUP>是与由以下组成的组中的一至五个相同或不同的基团：氢，卤素，C 1 -C 6 - 烷基，C 1 - C 1 -C 6 - 烷氧基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 卤代烷氧基 C 1 -C 4 - 烷硫基，C 1 -C 4 - 烷氧基烷氧基，C 1 -C 4烷基硫基，C 1 -C 4 - -C 6 - 烷基羰基; n为0-5; p取决于自由价格的数量，0-4。
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6.发明授权Benzophenones, the production thereof and their use for controlling plant pathogenic fungi 失效二苯甲酮，其生产及其用于控制植物致病真菌的用途公开(公告)号：US06919485B2
公开(公告)日：2005-07-19
申请号：US10469688
申请日：2002-03-09
申请人： Thomas Grote , Andreas Gypser , Joachim Rheinheimer , Ingo Rose , Peter Schäfer , Frank Schieweck , Norbert Götz , Karl Eicken , Eberhard Ammermann , Siegfried Strathmann , Gisela Lorenz , Reinhard Stierl
发明人： Thomas Grote , Andreas Gypser , Joachim Rheinheimer , Ingo Rose , Peter Schäfer , Frank Schieweck , Norbert Götz , Karl Eicken , Eberhard Ammermann , Siegfried Strathmann , Gisela Lorenz , Reinhard Stierl
摘要： The invention relates to benzophenones of formula (I), in which the substituents have the following meanings: X represents halogen; R1 represents hydrogen, halogen, C1-C6 alkyl, halo-C1-C2 alkyl, C1-C4 alkoxy, oxyhalomethyl or nitro, and; R2 represents hydrogen, C1-C6 alkyl, benzyl, cyclohexylmethyl or C3-C6 alkenyl. The invention also relates to the production of these benzophenones and to their use as fungicides
摘要翻译： 本发明涉及式（I）的二苯甲酮，其中取代基具有以下含义：X表示卤素; R 1表示氢，卤素，C 1 -C 6烷基，卤代C 1 -C 3 烷基，C 1 -C 4烷氧基，氧卤甲基或硝基，和; R 2表示氢，C 1 -C 6烷基，苄基，环己基甲基或C 3 -C 3 > 6个烯基。 本发明还涉及这些二苯甲酮的制备及其作为杀真菌剂的用途
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7.发明授权Benzamidoxime derivatives, intermediates and processes for their preparation, and their use as fungicides 失效苯甲酰胺肟衍生物，中间体及其制备方法及其作为杀真菌剂的用途公开(公告)号：US06680402B2
公开(公告)日：2004-01-20
申请号：US10261122
申请日：2002-10-01
申请人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Karl Eicken , Joachim Rheinheimer , Frank Wetterich , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
IPC分类号： C07C25549
CPC分类号： C07D333/24 , A01N37/52 , A01N43/10 , A01N43/56 , C07C255/53 , C07C255/54 , C07C259/18
摘要： Benzamidoxime derivatives of the formula I: where R1 is difluoromethyl or trifluoromethyl R2 is hydrogen or fluorine R3 is C1-C4-alkyl which may be substituted by cyano, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, C3-C8-cycloalkyl-C1-C4-alkyl R4 is phenyl-C1-C6-alkyl which may carry one or more substitutents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the phenyl ring, or is thienyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the thienyl ring, or is pyrazolyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the pyrazole ring, are prepared, and intermediates for their preparation and their use as fungicides are described.
摘要翻译： 式I的苯甲酰胺肟衍生物：其中R 1是二氟甲基或三氟甲基R 2是氢或氟，R 3是可以被氰基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基 - C 1 -C 4 - 烷基，C 3 -C 6 - 烯基，C 3 -C 6 - 卤代烯基，C 3 -C 6 - 炔基，C 3 -C 8 - 环烷基-C 1 -C 4 - 烷基R 4是苯基-C 1 -C 6 - 或更多的选自苯基环上的卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基的取代基，可以携带的噻吩基-C 1 -C 4烷基 一个或多个选自噻吩基环上的卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基的取代基，其可以是吡唑基-C 1 -C 4烷基， 在吡唑环上携带一个或多个选自卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和C 1 -C 4 - 卤代烷氧基的取代基，制备中间体和 描述了它们作为杀真菌剂的用途。
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8.发明授权公开(公告)号：US06346538B1
公开(公告)日：2002-02-12
申请号：US09581444
申请日：2000-06-13
申请人： Klaus Schelberger , Maria Scherer , Karl Eicken , Manfred Hampel , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Klaus Schelberger , Maria Scherer , Karl Eicken , Manfred Hampel , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
IPC分类号： A01N4342
CPC分类号： A01N43/40 , A01N43/42 , A01N37/52 , A01N2300/00
摘要： Fungicidal mixtures comprise as active components a) an amide compound of the formula I A—CO—NR1R2 I in which A, R1 and R2 are as defined in the description, and b) compounds of the formula II, their N-oxide or one of their salts where the substituents R12 to R18 are as defined in the description, and/or c) compounds of the formula III where the substituents X1 to X5 and R19 to R22 are as defined in the description, in a synergistically effective amount.
摘要翻译： 杀真菌混合物包含作为活性组分的a）式I的酰胺化合物，其中A，R 1和R 2如说明书中所定义，和b）式II化合物，其N-氧化物或其盐之一，其中取代基R12至 R 18如说明书中所定义，和/或c）式III化合物，其中取代基X1至X5和R19至R22如协商有效量所述，如说明书中所定义。
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9.发明申请Fungicidal mixtures based on amide compounds and morpholine or piperidine derivatives 有权基于酰胺化合物和吗啉或哌啶衍生物的杀真菌混合物公开(公告)号：US20080103144A1
公开(公告)日：2008-05-01
申请号：US11322211
申请日：2005-12-30
申请人： Klaus Schelberger , Maria Scherer , Karl Eicken , Manfred Hampel , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
发明人： Klaus Schelberger , Maria Scherer , Karl Eicken , Manfred Hampel , Eberhard Ammermann , Gisela Lorenz , Siegfried Strathmann
CPC分类号： A01N43/40 , A01N47/34 , A01N47/12 , A01N43/76 , A01N43/08 , A01N37/46 , A01N37/38 , A01N37/36 , A01N2300/00
摘要： Fungicidal mixtures comprise as active componentsa) an amide compound of the formula I A—CO—NR1R2 I in which A, R1 and R2 are as defined in the description, andb) dimethomorph or flumetover, and/orc) a valinamide of the formula III in which R13 is C3-C4-alkyl and R14 is naphthyl or phenyl, where the phenyl radical is substituted in the 4-position by a halogen atom, a C1-C4-alkyl or C1-C4-alkoxy group, and/or d) benalaxyl, ofurace, metalaxyl, furalaxyl or oxydixyl, and/ore) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylureain a synergistically effective amount.
摘要翻译： 杀真菌混合物包含作为活性组分的a）式I的酰胺化合物<？in-line-formula description =“In-line Formulas”end =“lead”→> A-CO-NR 1 其中A，R 1和R 2各自独立地表示：其中A，R 1，R 2， 2）如说明书中所定义，和b）烯酰吗啉或flumetover，和/或c）式III的缬氨酰胺，其中R 13是C 3
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10.发明申请公开(公告)号：US20060154924A1
公开(公告)日：2006-07-13
申请号：US11332221
申请日：2006-01-17
申请人： Klaus Schelberger , Maria Scherer , Reinhold Saur , Karl Eicken , Egon Haden , Eberhard Ammermann , Thomas Grote , Gisela Lorenz , Siegfried Strathmann
发明人： Klaus Schelberger , Maria Scherer , Reinhold Saur , Karl Eicken , Egon Haden , Eberhard Ammermann , Thomas Grote , Gisela Lorenz , Siegfried Strathmann
摘要： Fungicidal mixtures, comprising as active components a) a morpholine or piperidine derivative I selected from the group of the compounds Ia, Ib, Ic and Id b) compounds of the formula II where the substituents X1 to X5 and R1 to R4 are as defined below: X1 is C1-C4-haloalkyl, C1-C4-haloalkoxy or halogen; X2 to X5 are, independently of one another, hydrogen, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1-C4-haloalkoxy; R1 is C1-C4-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C4-alkyl-C3-C7-cycloalkyl, C1-C4-alkyl-C3-C7-cycloalkenyl, where these radicals may carry substituents selected from the group consisting of halogen, cyano and C1-C4-alkoxy, R2 is a phenyl radical or a 5- or 6-membered saturated or unsaturated heterocyclyl radical having at least one heteroatom selected from the group consisting of N, O and S, where the cyclic radicals may have one to three substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkoxy-C2-C4-alkenyl, C1-C4-alkoxy-C2-C4-alkynyl, R3 and R4 are, independently of one another, hydrogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-alkylthio, N-C1-C4-alkylamino, C1-C4-haloalkyl or C1-C4-haloalkoxy in a synergistically effective amount are described.
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